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窦房结在慢性睡眠限制大鼠中重构。

Sinoatrial node remodels in chronic sleep-restricted rats.

机构信息

a Histomorphometry and Stereology Research Center , Shiraz University of Medical Sciences , Shiraz , Iran.

b Department of Anatomy , Shiraz University of Medical Sciences , Shiraz , Iran.

出版信息

Chronobiol Int. 2019 Apr;36(4):510-516. doi: 10.1080/07420528.2018.1563900. Epub 2019 Jan 24.

Abstract

Chronic Sleep Restriction (CSR) is known as a risk factor for cardiovascular diseases. However, the structural changes of Sinoatrial (SA) node cells have received less attention. This study aimed to evaluate the effects of CSR on SA node in an animal model using stereological methods. Adult male Sprague-Dawley rats were randomly divided into CSR, grid-floor, and control groups. The CSR procedure was designed such a way that the animals had a full cycle of sleep (6 hours) per day, while they were unable to have a Rapid Eye Movement (REM) sleep during the remaining 18 hours. This was induced by a multiplatform box containing water. The grid-floor animals were placed in the same multiplatform box with a grid-floor covering to prevent falling in water. After 21 days, the right atria were dissected out. Then, the location of the SA node was determined and evaluated by stereological techniques. The total volume of the SA node, the total volume of the main node cells, the volume of the connective tissue, and mean volume of the node cells were respectively enlarged by 60%, 47%, 68%, and 51% in the CSR animals compared to the grid-floor rats (p < 0.05). However, no significant changes were detected in these parameters in the control and grid-floor animals. The population of the main node cells remained constant in all animal groups. In addition, the three-dimensional reconstruction of the SA node in the CSR group showed a hypertrophied appearance. In conclusion, CSR induced hypertrophic changes in the rats' SA node structures without alteration in the number of main node cells.

摘要

慢性睡眠限制(CSR)被认为是心血管疾病的一个风险因素。然而,窦房结(SA)细胞的结构变化受到的关注较少。本研究旨在使用体视学方法评估 CSR 对动物模型中 SA 节点的影响。成年雄性 Sprague-Dawley 大鼠被随机分为 CSR、网格地板和对照组。CSR 程序的设计方式是让动物每天有 6 小时的完整睡眠周期,而在其余 18 小时内,它们无法进行快速眼动(REM)睡眠。这是通过一个包含水的多平台盒子来实现的。网格地板动物被放置在同一个多平台盒子里,上面覆盖着网格地板,以防止掉进水里。21 天后,取出右心房。然后,通过体视学技术确定和评估 SA 节点的位置。与网格地板大鼠相比,CSR 动物的 SA 节点总容积、主节点细胞总容积、结缔组织容积和节点细胞平均容积分别增大了 60%、47%、68%和 51%(p<0.05)。然而,在对照组和网格地板动物中,这些参数没有明显变化。所有动物组的主节点细胞数量保持不变。此外,CSR 组的 SA 节点的三维重建显示出肥大的外观。总之,CSR 导致大鼠 SA 节点结构发生肥大性变化,而主节点细胞数量没有改变。

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